NANO SILVER TOOTHPASTE

Dosage form: paste
Ingredients: SODIUM MONOFLUOROPHOSPHATE 1.4g in 200g, SILICON DIOXIDE 14g in 200g, GLYCERIN 5g in 200g
Labeler: Nanowell Korea Inc
NDC Code: 45163-451

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Active Ingredients: Colloidal Silicon Dioxide, Sodium Monofluorophosphate, Sodium Chloride, Glycerin

Inactive Ingredients: D-Sorbitol Solution, Polyethylene Glycol 1500, Hydrated Silica, Carboxymethylcellulose Sodium, Chitosan, Sodium Alginate, Tocopherol Acetate, Xylitol, Saccharin Sodium, Methyl Parahydroxybenzoate, Sodium Lauryl Sulfate, Argentum, Mentha Oil, L-Menthol, Purified Water

Warnings: When using this product, do not use for sensitivity longer than four weeks unless recommended by a dentist.  Stop use and ask a dentist if the sensitivity problem persists or worsens.  Sensitive tooth may indicate a serious problem that may need prompt care.

Keep out of reach of children.  If accidentally swallowed, get medical help or contact a Poison Control Center right away.

Direction: adults and children 12 yrs and older.  apply at least a half-inch strip of the product onto a soft bristled toothbrush.  Brush teeth thoroughly for at least 3 minutes twice a day (morning and evening).  under 12 yrs ask a dentist.

NANO SILVER TOOTHPASTE 
sodium monofluorophosphate, silicon dioxide, glycerin paste
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:45163-451
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM MONOFLUOROPHOSPHATE (FLUORIDE ION) SODIUM MONOFLUOROPHOSPHATE1.4 g  in 200 g
SILICON DIOXIDE (SILICON DIOXIDE) SILICON DIOXIDE14 g  in 200 g
GLYCERIN (GLYCERIN) GLYCERIN5 g  in 200 g
Packaging
#Item CodePackage Description
1NDC:45163-451-63200 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35501/20/2010
Labeler - Nanowell Korea Inc (631151268)
Registrant - Nanowell Korea Inc (631151268)
Establishment
NameAddressID/FEIOperations
Nanowell Korea Inc631151268manufacture

Revised: 01/2010
 
Nanowell Korea Inc

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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